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1 HB15 represses secondary wall development in pith.
2 on of the lignin biosynthetic pathway in the pith.
3 YC2/3-dependent superoxide dismutases in the pith.
4 gnin also accumulated highly in the attacked pith.
5 ls) and neurophysiology (he was the first to pith a frog).
6                     He was also the first to pith a frog, concluding that piercing the spinal medulla
7  is accumulated only within the cells of the pith and peridermis layers (peel) of the tuber as it dev
8 e expression occurring in epidermal, cortex, pith and xylem tissue.
9 s) VIII, X, and XI in different parts (skin, pith, and seed) of the fresh and dried fruit of bitter m
10  formed first in the vessels surrounding the pith at stem water potentials of approximately -1.2 mega
11 ympathetically denervated by thoracic spinal pithing, cardiac chronotropic vagal tone was quantified
12 egulated in a thick wall variant with narrow pith cavity, mildly spiral growth, and flat and enlarged
13  plausible mechanism resulting in the narrow pith cavity, weak spiral growth but increased vascular b
14  stp-2d showing secondary wall thickening in pith cells (STP).
15 liana with secondary cell wall thickening in pith cells associated with ectopic deposition of lignin,
16 s had stronger PCD-associated signals in the pith cells compared to solid-stemmed lines, which sugges
17 onsible for the parenchymatous nature of the pith cells in dicotyledonous plants.
18  accumulation of secondary cell walls in the pith cells of the stp-2d mutant.
19  characterize the refilling of xylem fibers, pith cells, and vessels under both excised and in vivo c
20            In contrast, refilling of fibers, pith cells, and vessels was negligible in intact sapling
21 ry forces: fibers refilled more rapidly than pith cells, while vessel refilling was minimal.
22 ry for retaining primary walls in parenchyma pith cells.
23 f caffeoyl coenzyme A O-methyltransferase in pith cells.
24 ic resonance results revealed that lignified pith contains feruloyltyramine as an unusual lignin comp
25 urrence of conducting vascular tissue in the pith (CVTP) of tracheophytes is noteworthy.
26 ural porous materials such as bone, wood and pith evolved to maximize modulus for a given density.
27 n single perfused mesenteric microvessels in pithed frogs (Rana pipiens).
28 measured in single mesenteric capillaries of pithed frogs and anaesthetised rats as perfusion velocit
29 single mesenteric capillaries and venules of pithed frogs to determine whether the rate of increase i
30 n single perfused mesenteric microvessels of pithed frogs, we assessed wall strength from the critica
31 f single perfused mesenteric microvessels in pithed frogs.
32 f single perfused mesenteric microvessels in pithed frogs.
33 nd permeability of mesenteric capillaries in pithed frogs.
34 position were determined in rind (outer) and pith (inner) tissues throughout stem development.
35 kly or unpigmented tissues such as the curd, pith, leaf bases and shoot meristems, and cryptically in
36       Herbivore-induced, jasmonate-dependent pith lignification in Nicotiana attenuata plays a crucia
37 the inner parenchymal cells of the stem, the pith; lignin also accumulated highly in the attacked pit
38 llelic elp1 (ectopic deposition of lignin in pith) mutants with altered lignin deposition patterns.
39 osited in patches of parenchyma cells in the pith of both young and mature elp1 stems.
40      The ectopic deposition of lignin in the pith of elp1 stems was accompanied by an increase in the
41 s of cells with incomplete cell walls in the pith of inflorescence stems.
42 asal vascular bundles were identified in the pith of pedicels supporting the fruitlets with the lowes
43  of histodifferentiated cortex and medullary pith of the rachis and barb rami.
44 ve regulators of secondary wall formation in pith opens up the possibility of significantly increasin
45 in was ectopically deposited in the walls of pith parenchyma cells in addition to its normal depositi
46                    In forsythia and alfalfa, pith parenchyma cells next to the vascular cylinder were
47 bundles and interfascicular cells, and inner pith parenchyma cells with thin primary walls.
48 eaction, including sites around cells of the pith parenchyma, between the vascular elements, and with
49 at the growth displayed a spiral pattern and pith played an important role in promoting the primary t
50 odermal thickness, endodermal cell area, and pith radius were increased (7.53%, 21.1%, 63.3%, 61.4%,
51 hoxycurcumin are chiefly concentrated in the pith rather than the other parts of the turmeric rhizome
52 ge capacitance was associated with fiber and pith refilling as driven by capillary forces: fibers ref
53 In excised stems that were sealed, fiber and pith refilling was associated with vessel emptying, indi
54 sion showed increased stem diameter, reduced pith size, and significantly accelerated root regenerati
55 monstrate that NaMYC2 and NaMYC3 orchestrate pith-specific lignification in response to T. mucorea at
56                                              Pith-specific lignification induced by the stem-boring h
57  NaMYC2/3-mediated regulatory network in the pith that integrates monolignol biosynthesis, lignin pol
58 ylem sap and single parenchymal cells in the pith, thereby differentiating their chemical composition
59 stem-specific responses, particularly in the pith, to stem-boring herbivores.
60 ong NaMYC2/3-dependent genes in the attacked pith, we identify NaTHT1, responsible for synthesizing t
61 he avb1 stems abnormally penetrated into the pith, which resulted in a disruption in the ring-like ar
62                   MC was concentrated in the pith, with some presence in the bark.